Glycolytic ATP fuels the plasma membrane calcium pump critical for pancreatic cancer cell survival

Andrew D. James, Anthony Chan, Oihane Erice, Ajith K. Siriwardena, Jason I E Bruce

Research output: Contribution to journalArticlepeer-review


Pancreatic cancer is an aggressive cancer with poor prognosis and limited treatment options. Cancer cells rapidly proliferate and are resistant to cell death due, in part, to a shift from mitochondrial metabolism to glycolysis. We hypothesized that this shift is important in regulating cytosolic Ca 2+ ([Ca2+]i), as the ATP-dependent plasma membrane Ca2+ ATPase (PMCA) is critical for maintaining low [Ca 2+]i and thus cell survival. The present study aimed to determine the relative contribution of mitochondrial versus glycolytic ATP in fuelling the PMCA in human pancreatic cancer cells.Wereport that glycolytic inhibition induced profound ATP depletion, PMCA inhibition, [Ca 2+]i overload, and cell death in PANC1 and MIA PaCa-2 cells. Conversely, inhibition of mitochondrial metabolism had no effect, suggesting that glycolytic ATP is critical for [Ca2+]i homeostasis and thus survival. Targeting the glycolytic regulation of the PMCA may, therefore, be an effective strategy for selectively killing pancreatic cancer while sparing healthy cells. © 2013 by The American Society for Biochemistry and Molecular Biology, Inc.
Original languageEnglish
Pages (from-to)36007-36019
Number of pages12
JournalJournal of Biological Chemistry
Issue number50
Publication statusPublished - 13 Dec 2013


  • ATP
  • Calcium ATPase
  • Calcium signaling
  • Cell death
  • Glycolysis
  • Metabolism
  • PMCA
  • Pancreatic cancer
  • Warburg
  • calcium overload


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